Axelgaard Mfg. Co., Ltd. is one of 5134 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Axelgaard Mfg. Co., Ltd. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Axelgaard Mfg. Co., Ltd. has 11 FDA 510(k) cleared neurology devices. Based in Irvine, US.
Historical record: 11 cleared submissions from 1985 to 2014.
Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.
Axelgaard Mfg. Co., Ltd. — FDA 510(k) Products and Clearance History
11 devices
Cleared
Feb 13, 2014
PALS PLATINUM NEUROSTIMULATION ELECTRODES
Neurology
192d
Cleared
Jul 17, 2013
VALUTRODE NEUROSTIMLATION ELECTRODES
Neurology
99d
Cleared
Jun 18, 2008
COMFORT IONTOPHORESIS ELECTRODES/ BUFFERED IONTOPHORESIS ELECTRODE TREATMENT,...
Physical Medicine
107d
Cleared
Aug 22, 2002
ULTRASTIM KIT
Neurology
309d
Cleared
Jun 16, 2000
ULTRASTIM ELECTRODE, MODEL US4040
Neurology
85d
Cleared
Apr 13, 2000
PALS NEONATAL PEDIATRIC ECG ELECTRODE, MODELS PN100, PN200
Cardiovascular
83d
Cleared
Dec 18, 1998
EVERLAST NEUROSTIMULATION ELECTRODES 2X 2,MODEL # EL2020
Neurology
57d
Cleared
May 09, 1997
VALUETRODE
Neurology
94d
Cleared
Jan 28, 1988
TRANSCUTANEOUS ELECTRIC NERVE STIMULATION (TENS)
Neurology
87d
Cleared
Sep 22, 1987
TENS PALS PLUS
Neurology
54d
Cleared
Jun 18, 1985
ELECTRICAL NERVE STIMULATION(TENS) ELECTRODES
Neurology
21d